Characterization of New Proteomic Biomarker Candidates in Mucopolysaccharidosis Type IVA

Characterization of New Proteomic Biomarker Candidates in Mucopolysaccharidosis Type IVA

Mucopolysaccharidosis type IVA (MPS IVA) is a lysosomal storage disease caused by mutations in the <i>N</i>-acetylgalactosamine-6-sulfatase (<i>GALNS</i>) gene. Skeletal dysplasia and the related clinical features of MPS IVA are caused by disruption of the cartilage and its e...

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Bibliographic Details
Main Authors: Víctor J. Álvarez, Susana B. Bravo, Maria Pilar Chantada-Vazquez, Cristóbal Colón, María J. De Castro, Montserrat Morales, Isidro Vitoria, Shunji Tomatsu, Francisco J. Otero-Espinar, María L. Couce
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:International Journal of Molecular Sciences
Subjects:
biomarkers
enzyme replacement therapy
lysosomal disorders
proteomics
Online Access:https://www.mdpi.com/1422-0067/22/1/226

Internet

https://www.mdpi.com/1422-0067/22/1/226

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